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Completed Phase 3 Interventional

Study of Eszopiclone Compared to Placebo in the Treatment of Insomnia Secondary to Perimenopause/Menopause

ClinicalTrials.gov ID: NCT00366093

Public ClinicalTrials.gov record NCT00366093. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 6:56 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

The Efficacy of Eszopiclone 3 mg Compared to Placebo in the Treatment of Insomnia Secondary to Perimenopause or Menopause

Study identification

NCT ID
NCT00366093
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sumitomo Pharma America, Inc.
Industry
Enrollment
410 participants

Conditions and interventions

Conditions

Interventions

  • Eszopiclone Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
40 Years to 60 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2004
Primary completion
Dec 31, 2004
Completion
Dec 31, 2004
Last update posted
Feb 21, 2012

2004 – 2005

United States locations

U.S. sites
51
U.S. states
26
U.S. cities
51
Facility City State ZIP Site status
Not listed Mobile Alabama
Not listed San Diego California
Not listed Denver Colorado
Not listed Newington Connecticut
Not listed Aventura Florida
Not listed Clearwater Florida
Not listed Fort Meyers Florida
Not listed Gainesville Florida
Not listed Melbourne Florida
Not listed Miami Florida
Not listed Naples Florida
Not listed New Port Richey Florida
Not listed Pembroke Pines Florida
Not listed Tampa Florida
Not listed West Palm Beach Florida
Not listed Atlanta Georgia
Not listed Savannah Georgia
Not listed Arlington Heights Illinois
Not listed Champaign Illinois
Not listed Chicago Illinois
Not listed Lexington Kentucky
Not listed Louisville Kentucky
Not listed Boston Massachusetts
Not listed Brockton Massachusetts
Not listed Ann Arbor Michigan
Not listed St Louis Missouri
Not listed Lincoln Nebraska
Not listed Reno Nevada
Not listed Rochester New York
Not listed Cary North Carolina
Not listed Raleigh North Carolina
Not listed Winston-Salem North Carolina
Not listed Cleveland Ohio
Not listed Dayton Ohio
Not listed Mentor Ohio
Not listed Oklahoma City Oklahoma
Not listed Medford Oregon
Not listed Erie Pennsylvania
Not listed Philadelphia Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed Warwick Rhode Island
Not listed Columbia South Carolina
Not listed Cordova Tennessee
Not listed Houston Texas
Not listed Irving Texas
Not listed Sandy City Utah
Not listed Richmond Virginia
Not listed Renton Washington
Not listed Seatle Washington
Not listed Spokane Washington
Not listed Tacoma Washington

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00366093, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 21, 2012 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00366093 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →